KaryoNIM® Prenatal

Array CGH designed to detect genomic copy number variations at prenatal diagnosis

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Array CGH designed to detect the loss and gain of genome and chromosome regions responsible for up to 124 genetic syndromes associated with intellectual disability and congenital disorders. Specifically aimed at prenatal diagnosis, its powerful design reduces diagnostic complexity and improves the resolution of conventional karyotyping by up to 50 times in the critical regions of the syndromes being tested.

NIMGenetics offers QF-PCR (Quantitative Fluorescence Polymerase Chain Reaction) as a complementary test to KaryoNIM Prenatal, to rule out the presence of complete triploidy.

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